Coordinate clinical trial monitoring for ICON as a Bilingual Clinical Research Associate, applying medical data review and ICH-GCP knowledge. Travel approximately 60% as required.
As a CRA I, you will support clinical trial operations across ICON's clinical programmes. The position involves study start-up and monitoring activities, accurate documentation, and collaboration with stakeholders. You will help deliver high-quality outcomes while supporting patient safety and regulatory compliance.
Key Responsibilities:
- Coordinate study setup and monitoring activities independently
- Complete accurate study status reports and maintain documentation
- Manage sponsor-generated queries and support cost efficiency
- Build relationships with investigators, stakeholders, and site staff
- Ensure compliance with procedures, protocols, and requirements
Requirements:
- University degree in medicine, science, or equivalent
- Clinical trial monitoring experience
- Knowledge of ICH-GCP guidelines
- Expertise reviewing and evaluating medical data
- Willingness to travel approximately 60% as required
Apply clinical monitoring, medical data review, and stakeholder collaboration skills as a bilingual CRA supporting ICON studies.
Bilingual Clinical Research Associate in Ottawa employer: ICON Strategic Solutions
ICON Strategic Solutions is an exceptional employer located in the Greater Toronto Area, offering a dynamic work culture that prioritizes collaboration and innovation in clinical research. Employees benefit from extensive professional development opportunities, competitive compensation, and a supportive environment that values work-life balance, making it an ideal place for those looking to make a meaningful impact in respiratory and cardiovascular trials.
